ID   GM01252
AC   CVCL_V802
SY   GM-1252; GM 1252
DR   CLO; CLO_0030929
DR   BioSample; SAMN00803762
DR   Coriell; GM01252
DR   Wikidata; Q54836738
RX   CelloPub=CLPUB00447;
RX   DOI=10.5962/bhl.title.4090;
RX   PubMed=477407;
RX   PubMed=6617268;
CC   Population: African American.
CC   Cell type: Fibroblast; CL=CL_0000057.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   22Y
CA   Finite cell line
DT   Created: 16-04-14; Last updated: 29-06-23; Version: 11
//
RX   CelloPub=CLPUB00447;
RA   Mulivor R.A., Suchy S.F.;
RT   "1992/1993 catalog of cell lines. NIGMS human genetic mutant cell
RT   repository. 16th edition. October 1992.";
RL   (In misc. document) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda; USA (1992).
//
RX   DOI=10.5962/bhl.title.4090;
RA   Coriell L.L., Greene A.E.;
RT   "The human genetic mutant cell repository: list of genetic variants,
RT   chromosomal aberrations and normal cell cultures submitted to the
RT   repository. 4th edition. October 1977.";
RL   (In misc. document) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda; USA (1977).
//
RX   PubMed=477407; DOI=10.1159/000131367;
RA   Pope I.S., Thuline H.C., Aronson M.M., Bozarth B., Greene A.E.,
RA   Coriell L.L.;
RT   "Duplication of a segment of chromosome 3 in a subject with multiple
RT   congenital anomalies and a 47,XYY father, inversion of chromosomes 3
RT   and 9 in the mother, and inversion of chromosome 9 in a brother.
RT   Repository identification Nos. GM-1253, GM-1252, and GM-1251.";
RL   Cytogenet. Cell Genet. 24:127-128(1979).
//
RX   PubMed=6617268; DOI=10.1159/000131883;
RA   Aronson M.M., Nichols W.W., Mulivor R.A., Greene A.E., Coriell L.L.;
RT   "Breakpoint map of chromosomal inversion and deletion cell cultures in
RT   the NIGMS Human Genetic Mutant Cell Repository.";
RL   Cytogenet. Cell Genet. 35:298-302(1983).
//